510(k) K253436

Device
c-med0 alpha
Applicant
Cosinuss GmbH
510(k) number
K253436
Product code
MWI
Decision
Substantially Equivalent (SESE)
Decision date
2026-04-30
Date received
2025-10-01
Regulation
870.2300
Classification name
Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Ralph Heim
Address
Kistlerhofstrasse 60 Munich DE 81379 81379

FDA Registration Numbers

Source Documents

510(k) summary PDF

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